Canonical Allele Identifier: CA408405088
Gene: THBD HGNC NCBI

Linked Data

dbSNP Id: rs1268675176
MyVariant Identifiers: chr20:g.23028490T>C (hg19) chr20:g.23047853T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23047853T>C , CM000682.2:g.23047853T>C GRCh38
NC_000020.10:g.23028490T>C , CM000682.1:g.23028490T>C GRCh37
NC_000020.9:g.22976490T>C NCBI36
NG_012027.1:g.6812A>G , LRG_168:g.6812A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000377103.3:c.1652A>G MANE Select ENSP00000366307.2:p.Glu551Gly
ENST00000377103.2:c.1652A>G ENSP00000366307.2:p.Glu551Gly
NM_000361.2:c.1652A>G , LRG_168t1:c.1652A>G NP_000352.1:p.Glu551Gly
NM_000361.3:c.1652A>G MANE Select NP_000352.1:p.Glu551Gly
Search 100 bp 5'
Search 100 bp 3'